Benzyl Bromide → HCID 68465479, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([C:7]2([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:11][CH2:10][CH2:9][CH2:8]2)=[CH:3][CH:2]=1.[CH2:17](Br)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>C(#N)C>[CH2:17]([N:1]1[CH2:6][CH2:5][CH:4]([C:7]2([C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH2:11][CH2:10][CH2:9][CH2:8]2)[CH2:3][CH2:2]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Ethyl 1-pyridin-4-ylcyclopentanecarboxylate and benzyl bromide were reacted in acetonitrile under heating. The residue obtained by subjecting the reaction solution to evaporation under reduced pressure, triethylamine and platinum oxide were reacted in ethanol under a hydrogen atmosphere to obtain ethyl 1-(1-benzylpiperidin-4-yl)cyclopentanecarboxylate.
Workup
- temperatureunder heating
- customThe residue obtained
- customto evaporation under reduced pressure, triethylamine and platinum oxide
- customwere reacted in ethanol under a hydrogen atmosphere
Sources & evidence
- ORD record
- ord-3892a21d5c914053805c59f75c839f17
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07776897B2
Reaction notes
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